2,6-Dichloroaniline → 4-(4'-Amino-3',5'-dichlorobenzyl)-5-methylimidazole

HRID 325945Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 325945
Cl.Cl[CH2:3][C:4]1[N:5]=[CH:6][NH:7][C:8]=1[CH3:9].[Cl:10][C:11]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[C:12]=1[NH2:13]>C1(C)C(C)=CC=CC=1>[NH2:13][C:12]1[C:11]([Cl:10])=[CH:17][C:16]([CH2:3][C:4]2[N:5]=[CH:6][NH:7][C:8]=2[CH3:9])=[CH:15][C:14]=1[Cl:18]

Komponenten

4

Versuchsvorschrift

A mixture of 6.0 g of 4-chloromethyl-5-methylimidazole hydrochloride, 9.0 g of 2,6-dichloroaniline and 40 ml of xylene is refluxed with stirring for 3 hours. The mixture is then filtered and the precipitate is washed with xylene. The precipitate is dissolved in 50 ml of water and the pH is adjusted to 8. The solution is extracted with toluene (3×30 ml). The combined toluene extracts are washed with 10 ml of water and evaporated to dryness. The residue, which is crude 4-(4'-amino-3',5'-dichlorobenzyl)-5-methylimidazole, is converted to the hydrochloride in isopropanol with HCl-ethyl acetate. The free base is liberated from the hydrochloride in water with sodium hydroxide. The melting point of the base is 172°-175° C.

Aufarbeitung

  1. temperatureis refluxed
  2. filtrationThe mixture is then filtered
  3. washthe precipitate is washed with xylene
  4. dissolutionThe precipitate is dissolved in 50 ml of water
  5. extractionThe solution is extracted with toluene (3×30 ml)
  6. washThe combined toluene extracts are washed with 10 ml of water
  7. customevaporated to dryness
  8. customis 172°-175° C.

Quellen und Nachweise

ORD-Eintrag
ord-f7ff9b77edfb44b587fe5279bccc2fb6
Quelldatensatz
uspto-grants-1984_04
Patentnummer
US04443466

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